Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 10742-8902-01 recalled?

Red Cross Oral Pain Relief · 1 BOTTLE in 1 BLISTER PACK (10742-8902-1) / 3.7 mL in 1 BOTTLE

Yes — this exact package was recalled

1 FDA recall names the code 10742-8902-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
benzocaine
Strength
BENZOCAINE 200 mg/mL
Form
Liquid · Topical
Labeler
The Mentholatum Company
Type
Human OTC Drug
Product code
10742-8902

Recalls naming this package

Class III · Low risk

Red Cross Oral Pain

Labeling; Not Elsewhere Classified: The Mentholatum Company is initiating a voluntary recall due to an error in the labeling of the cotton pellet box found within the Red Cross Oral Pain blister pack. The cotton pellet box states that the product contains "Natural Eugenol Oil" in which it does not.

Terminated Labeling / mix-up The Mentholatum Company NDC 10742-8902-1 D-1541-2020

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler